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Vinorelbine Tartrate - 0703-4183-01 - (Vinorelbine Tartrate)

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Drug Information of Vinorelbine Tartrate

Product NDC: 0703-4183
Proprietary Name: Vinorelbine Tartrate
Non Proprietary Name: Vinorelbine Tartrate
Active Ingredient(s): 50    mg/5mL & nbsp;   Vinorelbine Tartrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Vinorelbine Tartrate

Product NDC: 0703-4183
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076028
Marketing Category: ANDA
Start Marketing Date: 20030301

Package Information of Vinorelbine Tartrate

Package NDC: 0703-4183-01
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (0703-4183-01) > 10 mL in 1 VIAL, SINGLE-USE

NDC Information of Vinorelbine Tartrate

NDC Code 0703-4183-01
Proprietary Name Vinorelbine Tartrate
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (0703-4183-01) > 10 mL in 1 VIAL, SINGLE-USE
Product NDC 0703-4183
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Vinorelbine Tartrate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20030301
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc.
Substance Name VINORELBINE TARTRATE
Strength Number 50
Strength Unit mg/5mL
Pharmaceutical Classes Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient]

Complete Information of Vinorelbine Tartrate


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